N-Boc-ethylenediamine hydrochloride

98%

Reagent Code: #72783
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CAS Number 79513-35-2

science Other reagents with same CAS 79513-35-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 196.68 g/mol
Formula C₇H₁₆N₂O₂HCl
badge Registry Numbers
MDL Number MFCD01076129
thermostat Physical Properties
Melting Point 148-151°C
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive compounds. It serves as a protecting group for amines, allowing selective reactions to occur without affecting the amine functionality. Commonly employed in peptide synthesis, where it helps in the stepwise construction of peptide chains. Also utilized in the development of drug candidates, especially in the modification of amine-containing molecules to enhance their stability or bioavailability. Its applications extend to the production of agrochemicals and fine chemicals, where precise control over chemical reactions is essential.

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Test Parameter Specification
Purity 98-100%
Infrared Spectrum Conforms to Structure
Appearance White to off-white powder crystals

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿390.00
inventory 5g
10-20 days ฿1,560.00
inventory 25g
10-20 days ฿6,680.00

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N-Boc-ethylenediamine hydrochloride
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Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive compounds. It serves as a protecting group for amines, allowing selective reactions to occur without affecting the amine functionality. Commonly employed in peptide synthesis, where it helps in the stepwise construction of peptide chains. Also utilized in the development of drug candidates, especially in the modification of amine-containing molecules to enhance their stability or bioavailabil

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive compounds. It serves as a protecting group for amines, allowing selective reactions to occur without affecting the amine functionality. Commonly employed in peptide synthesis, where it helps in the stepwise construction of peptide chains. Also utilized in the development of drug candidates, especially in the modification of amine-containing molecules to enhance their stability or bioavailability. Its applications extend to the production of agrochemicals and fine chemicals, where precise control over chemical reactions is essential.

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